This is an opportunity to be part of a dynamic team within the Engineering and Maintenance function. We
are looking for individuals who will support and drive Chanelle Pharma’s vision to be the most valued global
provider of high quality, competitively priced pharmaceutical products and to provide excellent services and
support to our customers.
Reporting to the Director of Engineering, the Project Engineer will apply strong
fundamental engineering expertise in support of design, commissioning and qualification of pharmaceutical
equipment and building utilities within our site. Effective management of projects ensuring compliance
with GMP and regulatory requirements. The role will add additional expertise to the engineering function
by supporting compliance with technical engineering reports.
KEY RESPONSIBILITIES:
1. Management and execution of engineering projects, encompassing capital projects, and equipment or
building changes to compliance to GMP standards.
2. Preparation/Review and execution of validation documentation such as URS/SDS/FAT/SAT/IQ/OQ/PQ
for various machinery/equipment/Utilities.
3. Management of projects to agreed timelines and costs, including capital facility and equipment
alterations and additions.
4. Ensure Project compliance with environmental, health and safety standards.
5. Ensure compliance to documented procedures and cGMP requirements are maintained to the highest
possible standards.
6. Achievement of KPIs as outlined in Performance and Development Plan.
7. Lead project assignments within multi-departmental scenarios.
8. Supervise outside contractors in compliance with company guidelines.
COMPETENCIES:
1. Organisational skills, personal efficiency, time management skills, and excellent communication skills.
2. Self-starter with demonstrated efficient work methods, analytical & problem-solving skills, and ability to
handle multiple tasks.
3. Ability to build relationships and collaborate with others is vital.
4. Demonstrate and lead on the values, initiatives, and culture of an organisation.
5. Professional expertise.
6. The above is not intended to be construed as an exhaustive list of all responsibilities, duties, and skills
required.
QUALIFICATIONS:
1. BS/Beng in Engineering or other technical discipline.
2. Minimum of 5 years engineering experience.
3. Experience in a cGMP Manufacturing and/or Biotechnology, pharmaceutical is required.
4. Ability to work on own and as part of a team.
5. Demonstrated initiative and self-starter.
6. Experience using the following is desirable - Project management software, AutoCAD, Excel.
PHYSICAL DEMANDS:
Health & Safety requirements (e.g., Manual Handling Training).
WORK ENVIRONMENT:
Office, Production, Workshop, Warehouse, Vendor Facilities.
Chanelle Pharma
Dublin Road, Loughrea,
Co Galway, Ireland.
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